The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation (Q48706853)

14 February 2018

title

The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation (English)

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14 February 2018

hereditary optic neuropathy

main subject

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N J Newman

1

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14 February 2018

M T Lott

series ordinal

2

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14 February 2018

D C Wallace

series ordinal

3

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language of work or name

English

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publication date

1 June 1991

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14 February 2018

American Journal of Ophthalmology

published in

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14 February 2018

volume

111

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issue

6

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14 February 2018

page(s)

750-762

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Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

cites work

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A mitochondrial DNA mutation as a cause of Leber's hereditary optic neuropathy

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Diagnosis of Leber's optic neuropathy by means of polymerase chain reaction amplification.

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Mitochondrial DNA mutation in family with Leber's hereditary optic neuropathy

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7 January 2021

Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathy.

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Rapid shift in genotype of human mitochondrial DNA in a family with Leber's hereditary optic neuropathy.

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Variable genotype of Leber's hereditary optic neuropathy patients.

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Mae III positively detects the mitochondrial mutation associated with type I Leber's hereditary optic neuropathy

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7 January 2021

Prevalence and predictors of rhabdomyolysis in patients with hypokalemia

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The molecular genetics of Leber's hereditary optic neuropathy

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7 January 2021

Mitochondria and Leber's hereditary optic neuropathy

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Leber's hereditary optic neuroretinopathy, a maternally inherited disease. A genealogic study in four pedigrees

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The early phase in Leber hereditary optic atrophy

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Ophthalmoscopic findings in Leber's hereditary optic neuropathy. II. The fundus findings in the affected family members

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Fundus findings in Leber's hereditary optic neuroretinopathy. III. Fluorescein angiographic studies

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Preliminary exclusion of an X-linked gene in Leber optic atrophy by linkage analysis

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Ocular Fundus in Acute Leber Optic Neuropathy

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LEBER'S DISEASE IN THE NETHERLANDS.

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The inheritance of Leber's disease. A genealogical follow-up study

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Leber's optic neuropathy: a clinical and visual evoked potential study of affected and asymptomatic members of a six generation family

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Bilateral optic neuropathy with remission in young men. Variation on a theme by Leber?

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Ophthalmoscopic findings in Leber's hereditary optic neuropathy. I. Fundus findings in asymptomatic family members

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A new manifestation of Leber's disease and a new explanation for the agency responsible for its unusual pattern of inheritance

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Leber's disease and dystonia: a mitochondrial disease

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7 January 2021

Neurological studies in families with Leber's optic atrophy

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7 January 2021

The heart in Leber's optic atrophy

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7 January 2021

Magnetic resonance imaging in Leber's optic neuropathy

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7 January 2021

Leber's optic neuropathy: clinical and visual evoked response studies in asymptomatic and symptomatic members of a 4-generation family

1 reference

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7 January 2021

New aspects of the genetic, etiologic, and clinical puzzle of Leber's disease

1 reference

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7 January 2021

Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy

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7 January 2021

10.1016/S0002-9394(14)76784-4

Identifiers

DOI

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14 February 2018